MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
22q11.2DS D004062
catch22 D004062
autosomal dominant opitz g bbb syndrome D004062
VCF syndrome D004062
sedlackova syndrome D004062
shprintzen syndrome D004062
syndrome, DiGeorge D004062
syndrome, VCF D004062
syndrome, sedlackova D004062
syndrome, shprintzen D004062
syndrome, velo-cardio-facial D004062
syndrome, velocardiofacial D004062
deletion syndrome, 22q11.2 D004062
familial third and fourth pharyngeal pouch syndrome D004062
conotruncal anomaly face syndrome (CTAF) D004062